Luteinizing hormone and testosterone response of sexually active and inactive rams.

The objective of this study was to identify rams exhibiting high (HP) and low (LP) levels of sexual performance and to determine whether their respective behavioral responses to ewes in estrus were related to changes in serum testosterone (T) and LH concentrations. Rams were selected on the basis of standardized serving capacity tests. Plasma T and LH concentrations in rams were measured in three experiments: 1) after 15 min of exposure to estrous ewes, 2) after an injection of 500 ng of LHRH, and 3) during an 11-h exposure to estrous ewes. During 15 min of exposure to ewes, HP rams were sexually active, whereas LP rams showed no sexual interest. Secretion of LH was similar (P greater than .05) between ram groups. Sexual arousal, copulation, and ejaculation of HP males were not related (P greater than .05) to LH secretion. Exposure to estrous ewes for 11 h, however, stimulated LH pulse frequency and elevated basal LH and T concentrations in HP but not LP rams (P less than .001). Luteinizing hormone secretion was positively correlated to the frequency of mounts (r = .19; P less than .01) and ejaculation (r = .17; P less than .03). Aggressive behavior of rams directed at ewes was negatively correlated to LH (r = -.22 P less than .003). Concentrations of LH and T after LHRH injection were similar between HP and LP rams (P greater than .05). These results show that the effects of the ewe on LH secretion of rams depend on length of the exposure period and sexual activity of the male.     

Behavior and endocrine changes in high-performing, low-performing, and male-oriented domestic rams following exposure to rams and ewes in estrus when copulation is precluded.

High-performing, low-performing, and male-oriented rams were used to investigate behavior and neuroendocrine correlates of sexual interest and discrimination. Treatment consisted of visual and olfactory contact with stimulus animals through a woven wire fence, which inhibited copulation (either ewes in estrus or other rams), for 4 h on each of three consecutive days. Before exposure to stimulus animals on d 1 and during the final 1 h of exposure on d 2, blood samples were collected every 15 min for 1 h to determine concentrations of LH and testosterone. During exposure to stimulus animals, rams were continuously observed and investigatory behaviors were recorded. There was no day effect for any behavior. Groups of rams differed (P < .05) in amounts of behaviors exhibited, but behaviors were not influenced by sex of stimulus animals. High-performing rams exhibited more (P < .05) investigatory behaviors toward stimulus animals than low-performing or male-oriented rams. Plasma concentrations of LH increased (P < .05) in high-performing rams following exposure to estrous ewes, but not following exposure to rams. In low-performing and male-orientated rams, concentrations of LH were unchanged regardless of sex of the stimulus animal. Change in plasma concentrations of testosterone from pre- to posttreatment did not differ between high-performing, low-performing, and male-oriented rams. However, low-performing rams exhibited an increase (P < .05) in plasma concentrations of testosterone following exposure to rams. In conclusion, high-performing rams exhibit a high degree of investigatory behaviors toward estrous ewes and other rams. High-performing rams seem to discriminate sex of stimulus animals and exhibit a neuroendocrine response (i.e., increased plasma LH) only when exposed to ewes in estrus. The sensory signals provided by estrous females are either not detected by low-performing or male-oriented rams or are not sufficiently provocative to elicit further investigation by these rams.     

Sexual performance of rams as determined by maturation and sexual experience

The purpose of this study was to compare the sexual performance of rams that differed in age (maturation) and sexual experience. Twenty-four ram lambs (8 mo of age) and 21 rams (20 mo of age) were individually exposed to four females in hormonally induced estrus for 30 min on five occasions, 7 d apart. Half (12) the ram lambs and nine of the yearlings were sexually naive at the start of testing (had been denied access to females since weaning); the remaining males were sexually experienced. The sexual performance of the virgin rams was poorer during the initial exposure to females than in subsequent tests, whereas the sexual behavior of the sexually experienced males did not change over the days of testing. Sexually naive ram lambs and rams exhibited an improvement in sexual performance between Tests 1 and 2; during Test 3 to 5 the sexual performance (ejaculations per test) of sexually naive and experienced rams was similar. The only effects of age (maturation) on sexual performance during the last three test days were a higher frequency of mounts without ejaculation plus mount attempts (P less than .03) and a greater number of mount interactions per ejaculation (P less than .02) by ram lambs. In conclusion, one or two relatively brief exposures to estrous females can bring the sexual performance of virgin rams up to levels comparable to that of experienced males. Also, ram lambs in good condition exhibit acceptable levels of sexual performance.     

Sexual performance of rams reared with or without females after weaning

The objective of this study was to determine the effect of postweaning exposure to females on the subsequent sexual performance of young rams. Twenty-five crossbred rams were reared in a group with ovariectomized females from 4.5 to 9 mo of age. Ewes were brought into estrus every 2 wk during this period. A companion group of 23 crossbred rams was not exposed to females following weaning. Four 30-min sexual performance tests were administered at 10 mo of age. Rams reared with males and females (RMF) exhibited more mounts (P less than .001) and more ejaculations (P less than .002) than rams reared only with males (RM). The frequency of successful matings by the latter group did not increase with experience. Nine rams were sexually inactive in the sexual performance tests. Follow-up tests revealed that two of the RMF rams and one RM ram developed and maintained a sexual preference for males. The six remaining rams eventually mated with females when tested in familiar pens and subsequently exhibited normal levels of sexual performance even when tested in an unfamiliar enclosure. Exposure to ewes during the postweaning prepubertal period enhanced sexual performance. However, early exposure to females did not ensure that all males developed sexual preferences for females. The environmental context in which sexual performance tests are administered may inhibit the expression of heterosexual behavior in a small percentage of animals. After heterosexual behavior was expressed, the rams continued to show normal levels of sexual performance.(ABSTRACT TRUNCATED AT 250 WORDS)     

Effect of morphine and naloxone on LH response and sexual behavior of rams (Ovis aries)

Effects of the opiate agonist, morphine, and antagonist, naloxone, on LH release, courtship behavior and ejaculation frequency of mature, sexually active or sexually inactive rams were investigated. Plasma LH concentrations were monitored from blood samples collected every 15 min for 10 hr (0800 to 1800 hr) from eight rams that were isolated from or in contact with estrous females. Plasma LH concentration was higher (P<.05) in sexually active rams exposed to receptive females compared with hormone concentration of rams isolated from ewes. Intravenous infusion of morphine sulphate (1 mg/kg) into rams 4 and 6 hr after exposure to ewes reduced (P<.05) plasma LH concentration as compared to rams given saline. Morphine did not affect (P>.05) courtship behavior (investigatory sniff, mount attempt, foreleg kick, flehmen, vocalization) but diminished (P<.05) number of ejaculations. In another trial, LH concentrations were higher (P<.05) in seven sexually active rams given naloxone iv or when given to three rams through an intracerebroventricular cannula (icv) as compared to LH response of sexually inactive rams. LH did not differ (P>.05) in seven sexually inactive rams before or after administration of naloxone. Investigatory sniffs by sexually active rams were increased (P<.03) after treatment with the opiate antagonist. Four of the seven sexually active rams had more ejaculations after naloxone compared with the pretreatment period, but mean ejaculation frequency after treatment did not differ (P=.31). Naloxone did not stimulate courtship behavior of sexually inactive males. These data suggest that the effect of opiates on sexual behavior and LH secretion depends upon the inherent level of sexual activity among rams.     

The effect of castration, estradiol and LHRH on LH secretion of lambs fed different levels of dietary energy

To examine the effect of diet on luteinizing hormone (LH) secretion, basal and luteinizing hormone releasing hormone (LHRH)-induced LH release was compared in intact or castrated-estradiol-17 beta implanted Finn-Dorset lambs. Ten to 12 wk old ram (n = 20) and ewe lambs (n = 20) were maintained under a 8L:16D photoperiod and fed for high (HG, 163 to 168 g/d) or low (LG, 76 to 103 g/d) rates of gain. Eight to 10 wk later, baseline LH concentrations were determined in blood samples collected at 20 min intervals for 7 h. The following day, lambs were given an iv injection of 5 micrograms of estradiol-17 beta followed within 4 h by LHRH (.5 or 2.5 micrograms). Baseline concentrations of LH for HG ewes were threefold greater than for LG ewes (4.2 vs 1.4 ng/ml), respectively. Time to peak response was inversely related to dietary energy level (P less than .025). Basal LH levels were similar across diets in rams. Total LH release following LHRH was dose-dependent (P less than .005). Effects of gonadal feedback were tested in a second group (n = 24) of castrated lambs. Changes in LH secretion were not different between diets within 3 to 4 wk after castration. A subcutaneous silastic implant (22 mm) of estradiol-17 beta inhibited (P less than .01) LH concentrations across diets in both ewes and rams. No differences in estradiol feedback on LH secretion (at the dose of steroid tested) were detected between HG and LG lambs. Within 8 d, however, basal LH concentrations were 60% lower (P less than .01) in HG vs LG ewes. Furthermore, peak LHRH-induced LH release was greater (P less than .025) in LG vs HG lambs of both sexes. Estradiol inhibited basal LH secretion in ewes and rams but facilitated LH release in lambs with a reduced rate of gain.     

Pulsatile or continuous infusion of luteinizing hormone-releasing hormone and hormonal concentrations in prepubertal beef heifers

An experiment was conducted to determine if exogenous luteinizing hormone-releasing hormone (LHRH) administered iv intermittently as pulses (P) or by continuous sc infusion (I) using osmotic minipumps could sustain pulsatile LH release and induce estrous cyclicity in prepubertal heifers. Prepubertal heifers were assigned randomly to: 1) receive pulses of LHRH (n = 6; 2.5 micrograms LHRH/2 h for 72 h), 2) be infused with LHRH (n = 11; 1.25 micrograms LHRH/h for 72 h), or 3) serve as controls (n = 16). Blood was collected at 20-min intervals for 8 h (0900 to 1700 h) from six heifers in each group on d 1, 2, 3 (during treatment), and on d 4 (during 8 h after terminating LHRH treatments). Heifers given LHRH had higher (P less than .01) LH concentrations than controls. Preovulatory-like LH surges occurred in three I, two P and no control heifers during treatment. Pulse frequencies of LH (no. LH pulses/8 h) were greater (P less than .001) for P heifers than for I and control heifers due to pulsatile LHRH treatment. Serum estradiol was higher (P less than .01) during treatment for LHRH-treated heifers than for controls. Serum follicle-stimulating hormone, cortisol, and progesterone were unchanged during treatment. High levels of cortisol on d 1 declined (P less than .001) to baseline by d 2. Characteristic progesterone rises or short luteal phases occurred within 10 d of treatment initiation in more (P less than .05) LHRH-treated heifers (I = 45%, P = 33%) than controls (6%), although days to first observed estrus and first ovulation were unaffected by treatments. Although both continuous and pulsatile administration of LHRH successfully induced LH and estradiol release as well as preovulatory-like LH surges in some heifers, earlier initiation of estrous cycles was not achieved. Estrous cycles appeared to be delayed by exposure to continuous LHRH infusions during the peripubertal period.     

Testosterone and luteinizing hormone responses to naloxone help predict sexual performance in rams

The first objective of this study was to determine whether LH and testosterone respond differently to a naloxone injection in relation to varying sexual performance in rams. If differences occurred, the second objective was to determine whether differences would predict variation in sexual performance. From a group of 1.5- to 3-yr-old rams, 20 sexually active and 39 sexually inactive rams were selected based on previously observed sexual behavior with estrual ewes. Each ram was exposed to three estrual ewes for 18 30-min sexual performance tests, and those found to be inactive were given two 30-min sexual partner preference tests. The final distribution was 28 sexually active, 22 inactive, and nine male-oriented rams. Rams were treated with 1.5 mg of naloxone/kg BW in December of Year 1 and again with either 0.75 or 1.5 mg of naloxone/kg BW in November of Year 2. Plasma concentrations of LH and testosterone were evaluated with mixed model analyses for repeated measures separately for each year to coincide with logistic procedures for modeling the probability that rams were sexually active. For Year 1, a sexual activity x age x time interaction for LH after naloxone was observed (P < 0.03). For testosterone, there was a sexual activity x time interaction (P < 0.03), with a similar, early increase for sexually active female-and male-oriented rams compared with a delayed, minimal increase for inactive rams. For Year 2, when all rams were over 2.5 yr of age, a sexual activity x time interaction for both LH and testosterone (P < 0.02) seemed more related to an earlier increase of both hormones for sexually active rams than the increase observed for inactive rams. In addition, sexually active rams had a greater increase in testosterone than inactive rams. No significant difference was observed between 0.75 and 1.50 mg of naloxone/kg BW. Testosterone and LH were used as explanatory variables and sexual activity was used as the response variable in logistic procedures. In Year 1, greatest prediction accuracy was 73.5% using testosterone at 60 min after naloxone injection. In Year 2, the greatest prediction accuracy was 85% using LH at 15 min multiplied by testosterone at 60 min after naloxone. Test repeatability for both years on the same rams was 76%. In conclusion, pattern and magnitude of naloxone-induced changes in endocrine function may facilitate identification of sexually active and inactive rams during the breeding season. Prediction accuracy of the naloxone-based test was 69 to 85%.     

Effect of prenatal androgenization on lamb performance, carcass composition and reproductive function

Two experiments were conducted in which pregnant crossbred ewes were randomly assigned to a control group or implanted with testosterone propionate/silastic implants between d 40 and d 60 of gestation. Implants contained approximately 2 g testosterone propionate and provided a constant delivery of 8.7 mg/d. Androgenized ewes (TE), born to implanted dams, had lower adjusted birth weights (P less than .05) than control ewes (CE) in both experiments. Treated rams (TR) also displayed lower birth weights than control rams (CR) in both experiments, but the difference was significant only in Exp. 2. Average daily gain was 16.4% more (P less than .05) for TE than for CE in Exp. 1. In Exp. 2, TE gained 9.6% faster (P less than .05) and had 14.6% (P less than .05) more weight per unit of feed consumed than CE. In both experiments, average daily gain and gain-to-feed ratio were similar for TR and CR. In Exp. 2, prenatal androgenization of ewes reduced (P less than .05) 12th rib fat thickness and decreased (P less than .05) percent kidney and pelvic fat. Yield grades of TE were lower than CE in both Exp. 1 (P less than .10) and Exp. 2 (P less than .05). From additional measurements taken in Exp. 2, liver weight per unit of carcass weight was greater (P less than .05), anogenital distance was greater (P less than .01) and test tube penetration into the vestibule was less (P less than .01) for TE than CE. The TE did not exhibit regular estrous cycles, while CE displayed recurring estrous cycles.     

Endocrine and body growth traits in heifers exposed to testosterone-propionate during early fetal development

This study was conducted to determine the effects of testosterone-propionate exposure during fetal development on sexual differentiation and growth rates in heifers. Ten pregnant cows were given subcutaneous injections of testosterone-propionate (250 mg/injection) every other day during d 40 to 60 of gestation. Four cows aborted after the end of testosterone treatment, while four heifers (androgenized females) and two bulls (androgenized males) were produced from the six remaining pregnant, testosterone-propionate treated cows. Calves from cows that did not receive exogenous hormone treatment were used as controls. At 8 mo of age, the androgenized heifers and control heifers and control steers were challenged with 1 mg estradiol-17 beta to induce a preovulatory luteinizing hormone (LH) surge. Two weeks later, pituitary responsiveness to exogenous luteinizing hormone releasing hormone (LHRH; 75 micrograms) was evaluated in androgenized heifers and in control heifers and control steers. To monitor growth rates, all animals were weighed at 28-d intervals from birth to 380 d of age. Androgenized females exhibited a partially masculinized phenotype as well as internal male reproductive structures. Treatment with estradiol-17 beta first depressed (P less than .05) serum LH concentrations in all animals, then induced (P less than .05) a preovulatory-like LH surge in control and androgenized females. Control steers did not (P greater than .05) exhibit a preovulatory-like LH surge following administration of estradiol-17 beta. Exogenous LHRH treatment stimulated peak LH concentrations (P less than .05) to a greater extent in control and androgenized females than in control steers.(ABSTRACT TRUNCATED AT 250 WORDS)     

Response to luteinizing hormone releasing hormone in postpubertal boars with large testes

The objective of the present study was to determine if postpubertal boars (12-13 months of age; 156 +/- 8 kg) with large testes had altered hypothalamic control of secretion of luteinizing hormone (LH). Seven boars with the highest estimated 150 d, paired testis weights from a line selected for large testes (769 +/- 60 g = mean weight of excised testes) and 8 boars from a control group (control, 544 +/- 20 g) were tethered in stalls and fitted with indwelling jugular catheters. Males were bled when they were intact, 14 days after castration and during administration of sodium pentobarbital anesthetic (subsequent to castration) to block secretion of endogenous LH-releasing hormone (LHRH). Blood samples were collected at 12-min intervals for 6 hr before and 1 hr after intravenous injection of LHRH in intact and castrated males. During anesthesia, LHRH was administered 4 times at 1-hr intervals and blood samples were collected every 6 min. All samples were analyzed for concentrations of LH and pooled samples were analyzed for concentrations of 17-beta estradiol (E2) and testosterone (T). In intact and castrated males, mean concentrations of LH, frequency and amplitude of pulses of LH, and concentrations of E2 and T were not different between boars of the two groups (P greater than .10). Response to exogenous LHRH was less (P less than .05) in intact males with large testes than in corresponding males from the control group (P less than .05). Fourteen days after castration, males that had larger testes before castration had less of a response to LHRH than males from the control group (P less than .05).(ABSTRACT TRUNCATED AT 250 WORDS)     

Use of naloxone challenge to predict sexual performance of young rams

The possibility of developing a hormone-based test to predict libido was evaluated using the response of LH and testosterone to naloxone. This test has been used to identify sexually active and inactive mature rams during the breeding season. The objective of this study was to determine whether the blood test could be used to detect differences in sexual activity of early postpubertal (29 +/- 0.1 wk) rams during the breeding season in November and again at 70 +/- 0.1 wk of age in August before the next breeding season. Rams were classed as sexually active or inactive using serving capacity tests (8 30-min observation periods to record sexual behaviors [mounts and ejaculations] of each ram individually exposed to three ewes in estrus) after the naloxone challenges. Naloxone (0.75 mg/kg of BW) was injected i.v. into 38 white-faced crossbred, 16 Polypay, and 49 Targhee rams. Blood samples were collected at 15-min intervals for 1 h before and 2 h after naloxone to measure LH and testosterone. Separate mixed-model analyses for repeated measures were used to analyze data for the same rams at 29 and 70 wk of age. Logistic regression procedures were used to model probabilities that rams were correctly predicted to be sexually active. A breed-type x sexual activity x time interaction for LH was observed (P < 0.05) after naloxone injection in 29-wk-old rams. At 70 wk of age, a breed-type x time interaction was detected (P < 0.001) for LH response to naloxone, but LH did not differ by sexual activity. At 29 wk of age, a breed-type x time interaction for testosterone response after naloxone was detected (P < 0.001), and at 70 wk of age, a sexual activity x time interaction was detected (P < 0.05) for testosterone after naloxone. Sexually active and inactive rams were not predicted accurately at 29 wk of age and were predicted 69 and 29% of the time for sexually active and inactive rams, respectively, at 70 wk of age. In conclusion, breed type at 29 and 70 wk of age can influence the naloxone challenge test, but the test cannot be used to discriminate between sexually active and inactive rams at 29 wk of age during the breeding season or at 70 wk of age immediately before the breeding season.     

Sexual performance of rams in serving capacity tests predicts success in pen breeding.

The purpose of this study was to determine the extent to which sexual performance (serving capacity) tests can be used to predict the sexual behavior and reproductive success of rams in the context of pen mating. Standard serving capacity tests were used to select four low (LP) and four high-performing (HP) rams from a population of 94 yearling males. Each selected ram was then exposed to approximately 30 estrus-synchronized ewes for a 9-d period. Ejaculations observed and mounting marks left on ewes confirmed the greater (P less than .001) sexual activity of the HP rams in the field. In addition, ewes exposed to HP rams had a higher lambing percentage, more lambs born, and more live lambs born per ewe. Ram classification was not related (P greater than .60) to the number of lambs born per ewe lambing (prolificacy). It was concluded that serving capacity tests, properly conducted, can be used to predict ram mating performance and thus aid in establishing more efficient ram-to-ewe stocking rates.     

Effects of melatonin and progesterone administered to ewes in spring and summer

Melatonin (MEL) was evaluated for effects on LH, prolactin (PRL) and fertility in spring (Exp. 1, 2) and summer (Exp. 3 to 5). In Exp. 1, 17 ovariectomized ewes bearing estradiol implants were fed 3 mg MEL or vehicle for 44 d beginning May 1. Melatonin decreased (P less than .001) PRL levels but had no effect on LH secretion and response to GnRH. In Exp. 2, 12 ewes each received a 40-d MEL ear implant or a sham implant on March 31. Progesterone-releasing pessaries (CIDR) were applied for 12 d and were withdrawn concomitant with ram joining on May 7. Neither treatment stimulated follicular development or induced estrus or ovulation. Exp. 3 and 4 were contemporary 2 x 2 factorial trials with 24 ewes at each of two locations. Melatonin implants were administered on June 29 and CIDR on July 22. The CIDR were removed and rams (Exp. 3, vasectomized; Exp. 4, fertile) were joined on August 3. Days from introduction of rams to estrus were reduced (P less than .05) by CIDR but not by MEL. All ewes lambed in Exp. 4, and days to estrus and conception were reduced (P less than .001) by CIDR but not by MEL. Exp. 5 was designed like Exp. 4 except that MEL implants were inserted June 20 and rams were joined August 8. Intervals from introduction of rams to estrus were reduced (P less than .01) by both MEL and CIDR treatments.(ABSTRACT TRUNCATED AT 250 WORDS)     

LHRH receptor, LH and FSH concentrations in anterior pituitaries of cycling, noncycling and early pregnant heifers

In domestic animals limited data are available concerning levels of pituitary luteinizing hormone-releasing hormone (LHRH) receptors during various physiological states. The objectives of this study were to quantify anterior pituitary gonadotropin and LHRH receptor concentrations in cycling, noncycling and early pregnant beef heifers. To accomplish these objectives, five heifers each were slaughtered, after synchronization with prostaglandin F2 alpha (PGF2 alpha), on d 0 (estrus), 7 and 14 of the estrous cycle and d 40 of pregnancy. Four heifers determined to be noncycling were also slaughtered. Pituitaries were collected and analyzed for LHRH receptor and gonadotropin concentrations. Pituitary luteinizing hormone (LH) concentrations were low on d 0 (1.4 +/- .2 micrograms/mg pituitary, mean +/- SE) and remained low on d 7 (1.4 +/- .1 micrograms/mg pituitary) before increasing (P less than .01) on d 14 (2.6 +/- .5 micrograms/mg pituitary). Luteinizing hormone concentrations, compared with d 0, were also elevated (P less than .01) in noncycling (NC; 2.6 +/- .2 micrograms/mg pituitary) animals and in 40-d pregnant (PG; 2.5 +/- .2 micrograms/mg pituitary) heifers. Pituitary follicle stimulating hormone (FSH) concentrations, though similar (P greater than .05) for all groups, paralleled changes in LH concentration. Pituitary LHRH receptor binding affinity did not differ (P greater than .05) among groups, with an overall Kd = .64 +/- .02 X 10(-9) M. Luteinizing hormone-releasing hormone receptor concentrations were highest on d 0 (1.09 +/- .12 fmol/mg pituitary) and fell (P less than .01) to low levels on d 7 (.75 +/- .11 fmol/mg pituitary).(ABSTRACT TRUNCATED AT 250 WORDS)     

Effects of melatonin on seasonal changes in reproduction of rams

Three studies were conducted to determine the effects of exogenous melatonin (M) on changes in scrotal circumference (SC), fertility and reproductive hormone concentrations of rams. Rams were initially housed in barns with controlled photoperiod and given 16 wk of long (16L:8D) or short (8L:16D) days. In Studies I and II, implants of M were given for 40 to 80 d beginning at maximal SC. Results showed that implanted rams had greater (P less than .05) blood M concentrations than nonimplanted controls. However, M did not prevent testicular regression. In Study III, M was given to rams after testicular regression had occurred. Rams were implanted with M weekly for 6 or 4 wk, followed by a withdrawal period of 4 wk (6:4, 4:4 respectively). Results showed that M (6:4) stimulated (P less than .05) testicular growth compared with nonimplanted controls. Treatment of rams with M for 8 mo did not affect LHRH-induced LH release (P greater than .05), but it reduced basal and LHRH-induced testosterone release (P less than .05). Reproductive performance of rams in Studies I and III was compared with that of nonimplanted rams. Fertility of M-treated rams in the spring from Studies I and III (86% to 91%) was similar to that in autumn (93%). Fertility of rams from Studies I and III exceeded (P less than .05) that of nonimplanted rams in April (59% to 62%). Net lamb production from ewes mated in the spring was greater if rams were treated with M and(or) photoperiod.     

Endocrine profiles, testicular gonadotropin receptors and sperm production in hemi-castrated ram lambs

The effects of hemi-castration upon compensatory hypertrophy, serum gonadotropin and testosterone concentrations, testicular gonadotropin receptors and daily sperm production (DSP) were studied in 10 crossbred ram lambs. At 4 mo of age lambs were either hemi-castrated (HC; n = 5) or left intact (INT; n = 5). Blood samples were collected every 2 h for the first 24 h post-surgery, every 6 h for the next 24 h and then three times weekly for the following 14 wk. Serial blood samples (15-min intervals for 8 h) were collected during the 4th, 8th and 12th week following hemi-castration. Individual mean testicular and epididymal weights increased (P less than .05) 48 and 33% in HC compared with INT rams, respectively. Serum follicle stimulating hormone (FSH) increased (P less than .05) within 8 h after HC, reached peak concentrations within 1 wk and remained elevated for 4 wk before returning to concentrations of INT rams. Neither mean serum luteinizing hormone (LH) nor pulse patterns of LH or FSH were different (P greater than .05) between these two groups at any period examined. Serum testosterone (T) concentrations were lower (P less than .05) during the first 48 h post-surgery in HC rams, but by 1 wk concentrations were similar (P greater than .05) to those in INT rams. Remaining testes from HC and INT rams were removed at 7 mo of age, 3 mo after initial gonadal manipulation. On a per-testis basis there were more (P less than .05) LH and FSH receptors in HC than INT rams, respectively; however, concentrations of receptors were not different (P greater than .05).(ABSTRACT TRUNCATED AT 250 WORDS)     

Sexual behavior of medium-ranked rams toward non-estrual ewes is stimulated by the presence of low-ranked rams

In sheep, access to receptive females is affected by dominance relationships. The aim of the first experiment was to determine how the presence of high- or low-ranking rams affects sexual behavior of medium-ranked rams toward non-estrual ewes in pen tests. A complementary objective was to determine whether the presence of 1 or 2 rams has stronger effects. Social rank of 13 rams was determined using the food competition test. The number of courtship behaviors, mounts, and ejaculations was recorded in pen tests with non-estrual restrained ewes. In the first experiment, medium-ranked rams were subjected to 5 tests with: (1) the ewe alone, (2) the ewe and 1 restrained tied high-ranked ram, (3) the ewe and 2 restrained tied high-ranked rams, (4) the ewe and 1 restrained tied low-ranked ram, and (5) the ewe and 2 restrained tied low-ranked rams. The number of high- or low-ranked rams (1 or 2) present in the tests did not affect the results. There were no differences on courtship behaviors, but the number of mounts and mounts with ejaculation was greater when low-ranked rams were present. In a second experiment, it was determined whether the presence of medium- or low-ranked rams stimulates sexual behavior of high-ranked rams. The high-ranked rams were tested with: (1) the ewe alone, (2) the ewe and 1 restrained tied medium-ranked ram, and (3) the ewe and 1 restrained tied low-ranked ram. No differences were recorded in relation to presence of other rams during the tests. It was concluded that the presence of low-ranked rams stimulates sexual behavior of medium-ranked rams toward non-estrual ewes in pen tests. This effect was not related with the number of rams included in the test. The presence of medium- or low-ranked rams did not alter the sexual behavior of high-ranked rams toward non-estrual ewes.     

Influence of castration and estrogen replacement on sexual behavior of female-oriented, male-oriented, and asexual rams

An experiment was conducted to determine whether exogenous estradiol-17beta (E2) could restore sexual behavior in castrated rams. The protocol consisted of three sequential 6-wk periods during which rams were studied while 1) intact, 2) bilaterally castrated, or 3) implanted s.c. with two 7.6-cm silastic implants each containing 309+/-16 mg of E2. Rams (classified as female-oriented [FOR, n = 7], male-oriented [MOR, n = 7], or asexual [n = 7]) were subjected to 30-min sexual behavior tests every 2 wk during the ensuing 18 wk. Rams were observed for mounts and ejaculations using two ovariectomized, estrous ewes and two intact males secured in stanchions. Behavioral data were analyzed using the signed rank test, but asexual rams showed no sexual behavior and therefore were not evaluated statistically. Jugular blood was collected prior to castration and at the end of the 18-wk period, and testicular venous (n = 21) and arterial (n = 8) bloods were collected immediately prior to castration. Radioimmunoassay was used to quantify systemic levels of estrone (E1), E2, and testosterone (T) and testicular serum concentrations of oxytocin (OT). Mounting behavior of MOR and FOR declined after castration (P < .05 and P < .10, respectively). Castration reduced the number of ejaculations by FOR (P < .05), but not by MOR (P > .10). Mounting behavior of castrated MOR and FOR was not affected by E2 treatment relative to that observed if castrated only (P > .10). Treatment of asexual rams with E2 did not stimulate sexual behavior in these rams. There were no marked differences (P > .10) among ram groups with regard to serum concentrations of E1, E2, or T prior to castration (overall mean +/- SE, 12.8+/-.7, 7.6+/-.5, and 2,670+/-780 pg/mL, respectively) or any difference (P > .10) in systemic concentration of E1 or E2 among ram groups after rams were implanted with E2 (overall mean +/- SE, 9.7+/-.7 and 9.0 +/-.7 pg/mL, respectively). Serum concentrations of E2 after implantation of the steroid did not differ from those present while rams were intact (P > .10). Testicular venous and arterial serum concentrations of OT were low and did not differ within or between rams. These results suggest that restoration of E2 concentrations to physiological levels in castrated adult rams (regardless of sexual orientation) cannot stimulate or reestablish sexual behaviors to levels observed prior to castration.     

LHRH antagonist decreases LH and progesterone secretion but does not alter length of estrous cycle in heifers.

The objective of this study was to evaluate the suppressive effect of an LHRH antagonist, Cetrorelix SB-75 (SB-75), on secretion of LH, FSH and ovarian function in beef heifers. In Exp. 1, heifers were treated with a single dose of 10 microg/kg body weight intramuscularly on d 3 of the estrous cycle. In Exp. 2, heifers received either a single injection (100 microg/kg) of SB-75 on d 3 of the estrous cycle or multiple injections of 20 microg/kg on d 3, 4, 5, 6, and 7. Serum LH, but not FSH, was suppressed from one to several days. However, neither FSH nor progesterone was significantly altered. In Exp. 3, heifers received an injection vehicle (5% mannitol) or 100 microg/kg BW of SB-75 on d 1 of the estrous cycle (30 h after first observed standing estrus). Injection of SB-75 suppressed LH pulse frequency on d 3, 5, and 7 (P < 0.001). The mean LH concentrations in the SB-75 treatment groups were lower on d 3 (P < 0.01) and 5 (P < 0.05). There were no differences (P > 0.1) between the two groups in the mean concentrations of LH on d 1, 7, or 14. Treatment did not affect the secretion pattern or concentration of FSH. Injection of SB-75 did not alter estradiol-173 concentrations (P > 0.1). Treatment reduced corpus luteum (CL) function as indicated by lower progesterone production. However, the length of the estrous cycle was not shortened. These data show that the CL can form and survive in the face of depressed LH concentrations during the early stages of the estrous cycle.